MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis

Background. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was...

Full description

Bibliographic Details
Main Authors: Silvia Méndez-Flores, Janette Furuzawa-Carballeda, Gabriela Hernández-Molina, Gustavo Ramírez-Martinez, Nora E. Regino-Zamarripa, Blanca Ortiz-Quintero, Luis Jiménez-Alvarez, Alfredo Cruz-Lagunas, Joaquín Zúñiga
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2019/5049245
id doaj-fc1886544ae944479aa474179b672d60
record_format Article
spelling doaj-fc1886544ae944479aa474179b672d602020-11-25T01:13:57ZengHindawi LimitedMediators of Inflammation0962-93511466-18612019-01-01201910.1155/2019/50492455049245MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its PathogenesisSilvia Méndez-Flores0Janette Furuzawa-Carballeda1Gabriela Hernández-Molina2Gustavo Ramírez-Martinez3Nora E. Regino-Zamarripa4Blanca Ortiz-Quintero5Luis Jiménez-Alvarez6Alfredo Cruz-Lagunas7Joaquín Zúñiga8Department of Dermatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoDepartment of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoDepartment of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoDepartment of Biochemistry, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoBackground. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was a cross-sectional study. We included 22 patients with subacute (SCLE) and 20 with discoid (DLE) lesions, and 19 healthy donors (HD). qRT-PCR for miRNA analysis, flow cytometry in peripheral blood, and skin immunohistochemistry were performed to determine the distribution of CD4 T cells and regulatory cells and their correlation with circulating miRNAs. Results. miR-150, miR-1246, miR-21, miR-23b, and miR-146 levels were downregulated in SCLE vs. HD. miR-150, miR-1246, and miR-21 levels were downregulated in DLE vs. HD. Peripheral CD4+/CD25-/IL-4+ cells and CD4+/CD25hi/Foxp3+ were negatively associated with miR-23b, and CD4+/CD25-/IFN-γ+ with miR-1246 in SCLE, whereas CD123+/CD196+/IDO+ cells were positively associated with miR-150 in DLE. In the tissue, CD4+/IL-4+ and CD20+/IL-10+ cells were positively associated with miR-21 and CD4+/IFN-γ+ with miR-31 in SCLE, whereas CD4+/IL-4+ cells were positively associated with miR-150, and CD20+/IL-10+ cells with miR-1246 and miR-146a in DLE. In the SCLE, lower miR-150 levels were correlated with higher CLASI scores. The KEGG pathway enrichment analysis revealed that cell cycle regulation pathways, p53, TGF-β, thyroid hormone, and cancer signaling pathways were shared between miR-21, miR-31, miR-23b, miR-146a, miR-1246, and miR-150. Conclusions. A downregulation of miR-150, miR-1246, and miR-21 in both CLE varieties vs. HD was determined.http://dx.doi.org/10.1155/2019/5049245
collection DOAJ
language English
format Article
sources DOAJ
author Silvia Méndez-Flores
Janette Furuzawa-Carballeda
Gabriela Hernández-Molina
Gustavo Ramírez-Martinez
Nora E. Regino-Zamarripa
Blanca Ortiz-Quintero
Luis Jiménez-Alvarez
Alfredo Cruz-Lagunas
Joaquín Zúñiga
spellingShingle Silvia Méndez-Flores
Janette Furuzawa-Carballeda
Gabriela Hernández-Molina
Gustavo Ramírez-Martinez
Nora E. Regino-Zamarripa
Blanca Ortiz-Quintero
Luis Jiménez-Alvarez
Alfredo Cruz-Lagunas
Joaquín Zúñiga
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
Mediators of Inflammation
author_facet Silvia Méndez-Flores
Janette Furuzawa-Carballeda
Gabriela Hernández-Molina
Gustavo Ramírez-Martinez
Nora E. Regino-Zamarripa
Blanca Ortiz-Quintero
Luis Jiménez-Alvarez
Alfredo Cruz-Lagunas
Joaquín Zúñiga
author_sort Silvia Méndez-Flores
title MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
title_short MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
title_full MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
title_fullStr MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
title_full_unstemmed MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
title_sort microrna expression in cutaneous lupus: a new window to understand its pathogenesis
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2019-01-01
description Background. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was a cross-sectional study. We included 22 patients with subacute (SCLE) and 20 with discoid (DLE) lesions, and 19 healthy donors (HD). qRT-PCR for miRNA analysis, flow cytometry in peripheral blood, and skin immunohistochemistry were performed to determine the distribution of CD4 T cells and regulatory cells and their correlation with circulating miRNAs. Results. miR-150, miR-1246, miR-21, miR-23b, and miR-146 levels were downregulated in SCLE vs. HD. miR-150, miR-1246, and miR-21 levels were downregulated in DLE vs. HD. Peripheral CD4+/CD25-/IL-4+ cells and CD4+/CD25hi/Foxp3+ were negatively associated with miR-23b, and CD4+/CD25-/IFN-γ+ with miR-1246 in SCLE, whereas CD123+/CD196+/IDO+ cells were positively associated with miR-150 in DLE. In the tissue, CD4+/IL-4+ and CD20+/IL-10+ cells were positively associated with miR-21 and CD4+/IFN-γ+ with miR-31 in SCLE, whereas CD4+/IL-4+ cells were positively associated with miR-150, and CD20+/IL-10+ cells with miR-1246 and miR-146a in DLE. In the SCLE, lower miR-150 levels were correlated with higher CLASI scores. The KEGG pathway enrichment analysis revealed that cell cycle regulation pathways, p53, TGF-β, thyroid hormone, and cancer signaling pathways were shared between miR-21, miR-31, miR-23b, miR-146a, miR-1246, and miR-150. Conclusions. A downregulation of miR-150, miR-1246, and miR-21 in both CLE varieties vs. HD was determined.
url http://dx.doi.org/10.1155/2019/5049245
work_keys_str_mv AT silviamendezflores micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT janettefuruzawacarballeda micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT gabrielahernandezmolina micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT gustavoramirezmartinez micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT noraereginozamarripa micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT blancaortizquintero micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT luisjimenezalvarez micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT alfredocruzlagunas micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
AT joaquinzuniga micrornaexpressionincutaneouslupusanewwindowtounderstanditspathogenesis
_version_ 1725159741910417408